and global regulatory submission publishing standards/formats (e.g. eCTD, EU CTR). Working knowledge of publishing tools (e.g... global regulatory submission projects. Provide submission and contribute to the technical related regulatory strategy...
-oriented Regulatory Affairs Associate who wishes to gain valuable hands-on experience across a variety of topics.... You will join our current Regulatory team and assist with regulatory lifecycle activities for specific products/customers on a global scale...
, reporting and publishing) in a global/matrix environment in pharmaceutical industry Working knowledge of the assigned disease...Job Description Summary The Associate Clinical Development Medical Director (Assoc. CDMD) is responsible for the...
experts it takes to enable our clients’ businesses to thrive. Whether it is providing global employment law advice, managing... a global IP portfolio or piecing together a multijurisdictional corporate transaction, we are able to have the right people...